NCT05410431

Brief Summary

Intraorbital epidermoid and dermoid cyst (DC) has been reported in the literature rarely. The current study evaluates clinicopathologic, radiologic, and management of intraorbital DC cases over ten years.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
9

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Jan 2010

Longer than P75 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2010

Completed
9.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2019

Completed
2.5 years until next milestone

First Submitted

Initial submission to the registry

May 31, 2022

Completed
8 days until next milestone

First Posted

Study publicly available on registry

June 8, 2022

Completed
Last Updated

June 8, 2022

Status Verified

June 1, 2022

Enrollment Period

9.9 years

First QC Date

May 31, 2022

Last Update Submit

June 4, 2022

Conditions

Outcome Measures

Primary Outcomes (3)

  • Histopathology report

    cyst pathology

    Ten years

  • Magnetic Resonance Imaging report

    The cyst features

    Ten years

  • Surgery technique

    Managing the cyst

    Ten years

Interventions

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients with Intraorbital Dermoid and Epidermoid Cyst

You may qualify if:

  • Those who had an excision biopsy with histology indicative of dermoid/epidermoid cyst

You may not qualify if:

  • Other cystic lesions

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

May 31, 2022

First Posted

June 8, 2022

Study Start

January 1, 2010

Primary Completion

December 1, 2019

Study Completion

December 1, 2019

Last Updated

June 8, 2022

Record last verified: 2022-06